Metabolic characterisation of THP-1 macrophage polarisation using LC-MS-based metabolite profiling

被引:47
|
作者
Abuawad, Alaa [1 ,2 ]
Mbadugha, Chidimma [3 ]
Ghaemmaghami, Amir M. [3 ]
Kim, Dong-Hyun [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Ctr Analyt Biosci, Div Adv Mat & Healthcare Technol, Nottingham, England
[2] Appl Sci Private Univ, Dept Pharmaceut Sci & Pharmaceut, Fac Pharm, Amman, Jordan
[3] Univ Nottingham, Sch Life Sci, Div Immunol, Fac Med & Hlth Sci, Nottingham, England
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”;
关键词
LC-MS; Macrophage polarisation; THP-1; cell; Metabolite profiling; Metabolic pathway analysis; NOVO SPHINGOLIPID BIOSYNTHESIS; IN-VITRO; ALTERNATIVE ACTIVATION; CELLS; CLEARANCE; ARGININE; LPS; IDENTIFICATION; INFLAMMATION; INDUCTION;
D O I
10.1007/s11306-020-01656-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Macrophages constitute a heterogeneous population of functionally distinct cells involved in several physiological and pathological processes. They display remarkable plasticity by changing their phenotype and function in response to environmental cues representing a spectrum of different functional phenotypes. The so-called M1 and M2 macrophages are often considered as representative of pro- and anti-inflammatory ends of such spectrum. Metabolomics approach is a powerful tool providing important chemical information about the cellular phenotype of living systems, and the changes in their metabolic pathways in response to various perturbations. Objectives This study aimed to characterise M1 and M2 phenotypes in THP-1 macrophages in order to identify characteristic metabolites of each polarisation state. Methods Herein, untargeted liquid chromatography (LC)-mass spectrometry (MS)-based metabolite profiling was applied to characterise the metabolic profile of M1-like and M2-like THP-1 macrophages. Results The results showed that M1 and M2 macrophages have distinct metabolic profiles. Sphingolipid and pyrimidine metabolism was significantly changed in M1 macrophages whereas arginine, proline, alanine, aspartate and glutamate metabolism was significantly altered in M2 macrophages. Conclusion This study represents successful application of LC-MS metabolomics approach to characterise M1 and M2 macrophages providing functional readouts that show unique metabolic signature for each phenotype. These data could contribute to a better understanding of M1 and M2 functional properties and could pave the way for developing new therapeutics targeting different immune diseases.
引用
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页数:14
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